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Progress in optics

III Multi-Photon Scattering Molecular Spectroscopy

S. Kielich

Published Jan 1, 1983• 32 citations
Publisher
DOI
10.1016/s0079-6638(08)70278-6

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Abstract Laser Stimulated Scattering and Multiphoton Excitation is the first book that comprehensively covers the following three major areas: (1) Quantum electrodynamic theory of stimulated scattering and multiphoton excitation processes; (2) Various stimulated scattering effects, including the early discovered stimulated Raman scattering (SRS) and stimulated Brillouin scattering (SBS), the later investigated stimulated Kerr scattering (SKS), and the recently developed stimulated Rayleigh–Bragg scattering (SRBS) and stimulated Mie scattering (SMS); (3) Multiphoton excitation-based nonlinear optical effects, photoelectric effects, atomic and molecular ionization effects, and molecular dissociation effects. Each chapter covers: (i) the concept and mechanism description, (ii) the necessary theoretical formulation, (iii) the experimental research achievements, and (iv) the scientific/technological applications. Laser Stimulated Scattering and Multiphoton Excitation is useful and suitable for academics, experts, and students working or interested in the areas of nonlinear optics, nonlinear photonics, laser spectroscopy, physical optics, physical chemistry, and optoelectronic engineering.
Absorption spectroscopy identifies molecules by detecting frequency-dependent optical loss, and its fundamental limit is a quantum channel-discrimination problem. In this work, we develop a general framework for characterizing the ultimate quantum limit of molecular absorption spectroscopy without collective measurements: we formulate it as an asymmetric quantum hypothesis testing task between different absorption channels. Using a semidefinite-programming formulation, we construct optimal probe states and compare them with coherent-state photon counting, Fock states, and two-mode squeezed vacuum probes. We introduce a random-loss channel model for imperfectly known background transmission, reflecting the fact that a blank experiment need not return all incident photons due to scattering, solvent absorption, or collection losses. Our results show that optimized non-classical probes can substantially outperform conventional laser spectroscopy, and that the advantage is robust to realistic baseline random loss. % In multi-frequency spectroscopy, the optimization also determines how photons should be allocated across absorption lines, revealing an additional resource-allocation advantage beyond single-mode state engineering. We illustrate our framework using infrared detection of 4-nitrophenol against chemically relevant comparison molecules, showing how quantum channel-discrimination methods provide constructive performance limits for molecular spectroscopy under realistic photon constraints.
Abstract This chapter focuses on spectroscopic applications of time dependent quantum mechanics focusing on molecular spectroscopy in condensed phases. (1) Molecular spectroscopy in the dressed state picture. (2) Resonance Raman scattering. (3) Resonance energy transfer. (4) Collective excitation and emission. (5) Thermal relaxation and dephasing (the Bloch equations, relaxation of a prepared state, dephasing (decoherence), the absorption lineshape, homogeneous and inhomogeneous broadening, motional narrowing, thermal effects in resonance Raman scattering). (6) A case study: Resonance Raman scattering and fluorescence from Azulene in a Naphthalene matrix. (7) Probing inhomogeneous bands (hole-burning spectroscopy, photon echoes, single-molecule spectroscopy. (8) Optical response functions.